使用基于毛细管的方法获取和组织微区转录组学分析。

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
Kaiqiang Ye, Yunxia Guo, Ying Wang, Jitao Xu, Qingyang Qin, Liyong He, Xi Yang, Yan Huang, Qinyu Ge, Xiangwei Zhao
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引用次数: 0

摘要

分析感兴趣微区(mris)的位点特异性转录组有助于对多细胞生物的全面了解。然而,简单有效地分离核磁共振成像用于空间检测基因表达仍然是一个挑战。在这里,我们开发了一种高效的基于毛细血管的显微解剖系统(CMS),用于从组织切片中精确分离目标样本。优化后的采样程序表明,CMS可以以97.9% %的效率进行mROI分离,并检测到足够数量的基因用于基因表达谱(CMS-seq)。我们应用CMS-seq揭示了阿尔茨海默病(AD)小鼠皮质区域和海马亚区的空间异质性。结果表明,CMS-seq可以在组织切片中分析空间转录组,并有望应用于空间多组学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acquisition and transcriptomic analysis of tissue micro-regions using a capillary-based method.

Profiling the site-specific transcriptomes of microregions of interest (mROIs) contributes to a complete understanding of multicellular organisms. However, the simple and efficient isolation of mROIs for spatially detecting gene expression remains challenging. Here, we develop an efficient capillary-based microdissection system (CMS) for precisely isolating targeted samples from tissue sections. Optimized sampling procedures reveal that CMS can perform mROI isolation with an efficiency of 97.9 %, and detect a sufficient number of genes for gene expression profiling (CMS-seq). We apply CMS-seq to uncover spatial heterogeneity in the cortex region of the mouse, and the subregions of hippocampus in an Alzheimer's disease (AD) mouse. Results demonstrate that CMS-seq can profile spatial transcriptomes in tissue sections and holds promise for application spatial multi-omics.

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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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